Canonical Allele Identifier: PA645459502
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg44His
CA4239718
NM_033507.3:c.131G>A